Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K013882 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Orasure Technologies Interept Benzodiazopene Miro-Plate EIA-Benzo EIA 2 plate Matrix Oral Fluid Coat... | 3 | 08/24/2020 | OraSure Technologies, Inc. |
| Orasure Technologies Interept Benzodiazopene Miro-Plate EIA-Benzo EIA 5plate Matrix Oral Fluid Coate... | 3 | 08/24/2020 | OraSure Technologies, Inc. |
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